FDA UDI In Commercial Distribution 🇺🇸 United States

Profound Matrix

DI: 07290109952949 · Model: FG71841 · Candela Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Profound Matrix
Primary DI
07290109952949
Version / Model
FG71841
Company Name
Candela Corporation
Labeler DUNS
053468385
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-15
Public Version
3
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
b62693e9-ef77-446c-8d77-5856a70bbbee

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
45220 Multi-modality skin surface treatment system

Identifiers

Type ID
Primary 07290109952949

Premarket Submissions

Submission Number Supplement Number
K211217 000